BACKGROUND
[0001] The statements in this section merely provide background information related to the
present disclosure and may not constitute prior art.
[0002] This disclosure relates to cement compositions and methods for designing the compositions.
[0003] During the construction of subterranean wells, it is common, during and after drilling,
to place a tubular body in the wellbore. The tubular body may comprise drillpipe,
casing, liner, coiled tubing or combinations thereof. The purpose of the tubular body
is to act as a conduit through which desirable fluids from the well may travel and
be collected, or fluids may be injected into the well. The tubular body is normally
secured in the well by a cement sheath.
[0004] The cement sheath is placed in the annular region between the outside of the tubular
body and the subterranean borehole wall by pumping the cement slurry down the interior
of the tubular body, which in turn exits the bottom of the tubular body and travels
up into the annulus. The cement slurry may also be placed by the "reverse cementing"
method, whereby the slurry is pumped directly down into the annular space.
[0005] The cement sheath provides mechanical support and hydraulic isolation between the
zones or layers that the well penetrates. The latter function is prevents hydraulic
communication between zones that may result in contamination. For example, the cement
sheath blocks fluids from oil or gas zones from entering the water table and contacting
drinking water. In addition, to optimize a well's production efficiency, it may be
desirable to isolate, for example, a gas-producing zone from on oil-producing zone.
The cement sheath achieves hydraulic isolation because of its low permeability. In
addition, intimate bonding between the cement sheath and both the tubular body and
borehole prevents leaks.
[0006] Cement slurry preparation may be performed by either batch mixing or continuous mixing.
During batch mixing, the cement slurry ingredients arc combined in a tank that provides
sufficient agitation to form a homogenous mixture. The tank may be sufficiently large
to accommodate the entire sluny volume to be placed in the well, or the required slurry
volume may be prepared in more than one tank. Continuous (or "on-the-fly") mixing
is a process during which the liquid and solid components of the slurry arc combined
and exposed to a high-shear environment to form a homogeneous mixture. The slurry
is immediately pumped into the well. Thus, the slurry is formed at a rate equal to
the pumping rate. Continuous mixing is logistically advantageous because less time
is required to prepare the slurry, and the process avoids the preparation of an excess
slurry volume that the operator would have to dispose of.
[0007] The intense shear environment associated with continuous mixing may cause air entrainment
and slurry foaming. A jet mixer may be used in which a regulated flow of solids into
the mixer is obtained by creating a void that sucks the dry powder into the mixing
fluid stream by the venturi effect. Any air entrainment should be removed before the
slurry is pumped downhole. Excessive slurry foaming may have several undesirable consequences.
Slurry gelation may result, and loss of hydraulic pressure during pumping may occur
owing to cavitation in the mixing system. In addition, air entrainment may cause higher-than-desired
slurry densities. During slurry mixing a densitometer is used to help field personnel
proportion the ingredients. If air is present in the slurry at the surface, the density
of the system "cement + water + air" is measured. Because the air becomes compressed
downhole, the densitometer may underestimate the true downhole slurry density. More
information concerning cement slurry mixing in the context of well cementing may be
found in the following publication.
Leugemors E. Metson J, Pessin J-L, Colvard RL, Krauss CD and Plante M: "Cementing
Equipment and Casing Hardware," in Nelson EB and Guillot D (eds.): Well Cementing-2nd
Edition, Houston, Schlumberger (2006) 343-362.
[0008] To minimize air entrainment and foaming, antifoam agents may be added to the mixing
fluid or dry blended with the cement solids. Antifoam agents produce a shift in surface
tension, alter the dispersibility of solids, or both, so that the conditions required
to produce a foam are no longer present
[0009] In well cementing, two classes of antifoam agents are commonly used: polyglycol ethers
and silicones. In current practice one type of antifoam agent is used (i.e., either
polyglycol ethers or silicones) in a particular cement slurry. Very small concentrations
may achieve adequate foam prevention, often lower than 0.1% by weight of water (BWOW).
Indeed, untifoam agents tend to be used sparingly, not only for economic reasons,
but also because adding excessive amounts of antifoam agents may actually stabilize
a foam and make the problem worse.
[0010] Polypropylene glycol (PPG) is most frequently used because of its lower cost and
effectiveness in most situations; however, optimal results are obtained when PPG is
added to the system before mixing. The silicones are highly effective antifoaming
and defoaming agents. They are often suspensions of finely divided silica particles
dispersed in polydimethylsiloxane or similar silicones. Unlike the polyglycol ethers,
silicones can destroy a foam regardless of when they are added to the system.
[0011] In recent years, new cementing technologies have been introduced wherein high concentrations
of organic polymer particles are present in cement slurries. Such particles may be
used to impart set cement flexibility. Or, the particles may be used to form so-called
self-healing cements. Various organic polymers may swell in the presence of wellbore
fluids such as hydrocarbons, carbon dioxide or hydrogen sulfide. If the cement sheath
fails during the well's lifetime, polymer swelling upon exposure to one or more of
the wellbore fluids may seal cracks or voids in the cement sheath, thereby restoring
zonal isolation.
[0012] Many of the organic polymers arc hydrophobic and may be difficult to incorporate
in the cement slurry during continuous mixing. This may cause excessive air entrainment.
This problem may be further exacerbated by the presence of latexes that are used to
prevent wellbore problems such as annular fluid migration. Also, water soluble polymers
may be added to impart fluid-loss control. Such additives may increase mixing fluid
viscosity, favoring the creation of more stable foams.
[0013] To further minimize the air entrainment and foaming problems, new cementing equipment
has been developed. For example, the Slurry Air Separator (SAS), developed by Schlumberger,
uses the hydrocyclone principle to separate entrained air from the cement slurry during
the mixing process. Nevertheless, when high concentrations of hydrophobic particles
are present, mixing difficulties may still persist. Under these circumstances it may
not be possible to perform continuous mixing at a reasonable rate.
[0015] EP2363428 discloses rheology modifiers including anti-foaming agents for cement slurries for
application in well-cementing operations.
SUMMARY
[0016] In an aspect, embodiments relate to well cementing compositions. The compositions
comprise an aqueous fluid, a solid blend comprising portland cement and an air entrainment
suppressing agent that comprises a blend of a silicone and a polypropylene glycol,
or a silicone that is functionalized with ether groups and hydrophobic particles as
defined by the claims.
[0017] In a further aspect, embodiments relate to methods for preparing a well cementing
composition as defined by the claims. An air entrainment suppressing agent is added
to an aqueous fluid, thereby forming a mixing fluid. The air entrainment suppressing
agent comprises a blend of a silicone and polypropylene glycol, or a silicone that
is functionalized with ether groups. The mixing fluid is combined with a solid blend
comprising portland cement in a continuous process, thereby forming a slurry.
[0018] Methods for cementing a subterranean well are shown. An air entrainment suppressing
agent is added to an aqueous fluid, thereby forming a mixing fluid. The air entrainment
suppressing agent comprises a blend of a silicone and polypropylene glycol, or a silicone
that is functionalized with ether groups. The mixing fluid is combined with a solid
blend comprising portland cement in a continuous process, thereby forming a slurry.
The slurry is then placed in the well.
[0019] Methods for measuring air entrainment in a composition. are shown. A rotational blade
mixer with a container is provided. An air entrainment suppressing agent is added
to an aqueous fluid, thereby forming a mixing fluid with a known density and volume.
The mixing fluid is placed in the container. A first rotational speed is chosen that
is between 2000 and 12,000 RPM. The mixer is operated for a time period sufficient
to expose the mixing fluid to at least 30.000 blade revolutions. Then, maintaining
the first rotational speed, a solid blend comprising portland cement is placed in
the container. The blend has a known density and absolute volume. The time required
for the blend to be dispersed homogeneously in the mixing fluid is recorded. The mixer
is then operated for 35 seconds at a second rotational speed of 12,000 RPM, thereby
forming a slurry. Within one minute after the slurry has been formed, a slurry density
measurement is performed with a mud balance at atmospheric pressure. The measured
slurry density is then compared with a theoretical slurry density calculated from
the known densities and volumes of the mixing fluid and solid blend.
[0020] This summary is provided to introduce a selection of concepts that are further described
below in the detailed description.
DETAILED DESCRIPTION
[0021] In the following description, numerous details are set forth to provide an understanding
of the present disclosure.
[0022] In this disclosure, Applicant discloses improved air entrainment suppressing agents
that arc particularly useful when preparing cement slurries that contain high concentrations
of hydrophobic particles. The air entrainment suppressing agents may comprise a blend
of a silicone and propylene glycol, or a silicone that is funcfionalized with ether
groups. The functionalized silicones may have a linear structure

or a branched structure

The ether groups may be characterized as a group (OC
3H
6)
b(OC
2H
4)
aO(CH
2)
c, wherein a has a mean value between 0 and 16, b has a mean value between 0 and 12
and c is a number between 1 and 6, provided that a + b ≥ 1. The group may be grafted
on the silicone backbone chain or used as mono- or di-terminal groups.
[0023] For each aspect, the aqueous fluid may be fresh water, tap water, sea water, produced
water or brines.
[0024] For each aspect, the silicone/propylene glycol blend may be present at a weight ratio
between 80% silicone/20% polypropylene glycol and 20% silicone/80% polypropylene glycol.
The polypropylene glycol may have a molecular weight between 1000 g/mol and 4000 g/mol,
or between 2000 g/mol and 4000 g/mol. The silicone/polypropylene blend may be present
in the composition at a concentration between 4 L/tonne of solids in the composition
and 40 L/tonne of solids in the composition, or between 10 L/tonne of solids in the
composition and 30 L/tonne of solids in the composition. In this disclosure the solids
in the composition may also be referred to as the "blend."
[0025] For each aspect, the functionalized silicone may be present at a concentration between
2 L/tonne of blend and 35 L/tonne of blend, or between 6 L/tonne of blend and 25 L/tonne
of blend.
[0026] For each aspect, the composition may further comprise latexes or water soluble polymers
or combinations thereof.
[0027] For each aspect, the hydrophobic particles comprise one or more members selected
from the group consisting of rubber particles, polyamides, polypropylene, acrylonitrile
butadiene rubbers, polyethylene, styrene butadiene, uintaite (also known by the commercial
name GILSONITE), styrene isoprene styrene (SIS) rubber, styrene isoprene copolymers,
styrene butadiene styrene (SBS) rubber, styrene divinylbenzene, fluoroelastomers,
perfluoroclastomers, polyphenylene sulfide, polyether-etherketones, petroleum coke
derivatives and coal. The hydrophobic particles may be present in a particle size
range between 1 and 2000 micrometers, or between 50 and 1000 micrometers or between
80 and 850 micrometers. The hydrophobic particles may be present at a concentration
between 10% by volume of blend (BVOB) and 55% BVOB, or between 15% BVOB and 40% BVOB.
The hydrophobic particles may present in granular or fibrous form, or both.
[0028] For each aspect, the latexes may comprise styrene butadiene latexes, carboxylated
styrene butadiene latexes, styrene acrylic latexes, acrylic latexes, isoprene latexes
or natural rubber latexes or combinations thereof. The latexes may be present in the
composition at concentrations between 35 and 500 L/tonne of blend, or between 80 and
350 L/tonne of blend, or between 80 and 300 L/tonne of blend.
[0029] For each aspect, the water soluble polymers may comprise cellulosic ethers, acrylates,
polymers containing 2-acrylamido-2-methylpropane sulfonic acid (AMPS) and acrylamides.
polysaccharides, polyvinyl alcohols, or crosslinked polyvinyl alcohols or combinations
thereof. The polymers may be present in the composition at concentrations between
0.01% and 2.0% by weight of solids (BWOS), or between 0.015% and 1.5% BWOS, or between
0.02% and 1.3% BWOS.
[0030] For cementing a subterrancan well, the slurry may be placed in the well during a
primary cementing of a remedial cementing operation.
[0031] For the method for measuring air entrainment in a composition, the rotational blade
mixer has a capacity of about one liter. Commercial examples of such mixers are WARING
blenders (available from Conair Corporation, Stamford, CT) and the Model 3260 Constant
Speed Mixer (available from Chandler Engineering, Broken Arrow, OK).
[0032] For the method for measuring air entrainment in a composition, solid blend may be
added to the container within a time period shorter than 2 minutes or shorter than
1 minute. The time period is defined as the time necessary for the solids to be poured
into the container and integrated within the liquid phase. In other words, no dry
solids or lumps should be observed in the slurry after the time period. Time periods
longer than two minutes are possible but not considered by Applicant to be a successful
result.
[0033] For the method for measuring air entrainment in a composition, the mud balance may
be an atmospheric mud balance or a pressurized mud balance.
[0034] For each aspect, the composition may further comprise extenders, weighting agents,
lost-circulation materials, fibers, dispersants, fluid-loss additives, antifoam agents,
strength retrogression prevention additives, gas migration control agents, surfactants
and gas generating agents.
[0035] The foregoing is further illustrated by reference to the following examples, which
are presented for purposes of illustration and are not intended to limit the scope
of the present disclosure.
EXAMPLES
[0036] Cement slurries were prepared and tested according to the method described herein
by Applicant, which differs from the recommended procedure published by the American
Petroleum Institute (API RP10B). The API procedure specifies operating the mixer at
4000 RPM while the solids are added to the container, then increasing the speed to
12,000 RPM for 35 seconds. The mixing device was a Model 3260 Constant Speed Mixer.
Unless indicated otherwise, the cement used in the examples was Dyckcrhoff Class G.
The cement slurries were prepared with tap water.
[0037] In these examples, Applicant chose an initial rotational speed of 4000 RPM and stirred
the mixing fluid in the container for a time period of 10 minutes, thereby exposing
the mixing fluid to 40,000 blade revolutions. Then, the mixing speed was increased
to 12,000 RPM for 35 seconds.
EXAMPLE 1
[0038] A test cement design (Flex 1) is shown in Table 1.

[0039] In the Flex 1 blend, the hydrophobic particles were composed of acrylonitrile-butadiene
rubber, present at a particle size range between 100 micrometers and 600 micrometers.
Silica as a strength retrogression prevention agent was present in the form of both
coarse crystalline particles having a particle size between 30 micrometers and 250
micrometers, and microfine amorphous particles having a particle size between 0.1
and 5.0 micrometers. The weight ratio of coarse to microfine silica was 2:1. The antifoam
agent was a silicone or polypropylene glycol or both. The antifoam agent concentration
was held constant at 4.45 L/tonne. The antisettling agent was a saccharide biopolymer.
The retarder was a lignosulfonate. The gas migration additive latex was styrene butadiene
latex. The weighting agent was Mn
3O
4, also known as the mineral hausmannite. With regard to the solid blend, a skilled
person will appreciate that the foaming problem arises from the presence of the hydrophobic
particles. The composition and particle size distribution of the cement and other
solid additives have a lesser role in the context of foaming.
[0040] The results of a series of mixing tests are shown in Table 2. The blend addition
time is listed as well as the slurry density measured with an atmospheric mud balance.

[0041] The results show that high concentrations of both antifoam agents were required to
achieve a slurry density improvement. None of the compositions was able to achieve
a slurry density equal to the theoretical slurry density of 2000 kg/m
3. Nevertheless, these tests confirm a synergistic effect when both antifoam agents
are present.
[0042] A comparative test was also performed wherein the standard API mixing procedure was
employed. The measured slurry density after mixing was 1990 kg/m
3. Thus, the standard API mixing procedure did not detect the foaming problem.
EXAMPLE 2
[0043] Two test designs (Flex 2 and Flex 3) are shown in Table 3.

[0044] The solid blends for Flex 2 and Flex 3 were the same as that of Flex 1 in Example
1: however, the mixing fluid compositions were different. The dispersant and retarder
were based on lignosulfonates, and the fluid loss control additive was an AMPS/acrylamide
copolymer.
[0045] The results of a series of mixing tests with the Flex 2 composition are shown in
Table 4.
Table 4. Blend addition times and slurry density measurements from Flex 2 compositions.
| Test |
Silicone Antifoam (L/tonne) |
Polypropylene Glycol (MW = 4000) (L/tonne) |
Blend Addition Time (s) |
Measured Slurry Density (kg/m3) |
| 2A |
26.7 |
- |
59 |
1780 |
| 2B |
- |
26.7 |
55 |
1840 |
| 2C |
13.35 |
13.35 |
50 |
1850 |
[0046] In Tests 2A-2C, the total antifoam concentration was held constant at 26.7 L/tonne.
As observed in Example 1, the combination of silicone and glycol antifoams was synergistic
in terms of the blend addition time and the measured slurry density. A comparative
test was performed using the API mixing procedure. The measured slurry density was
1860 kg/m
3.
[0047] The results of a series of mixing tests with the Flex 3 composition are shown in
Table 5.
Table 5. Blend addition times and slurry density measurements from Flex 3 compositions.
| Test |
Silicone Antifoam (L/tonne) |
Polypropylene glycol (L/tonne) |
Blend Addition time (s) |
Measured Slurry Density (kg/m3) |
| 2D |
4.45 |
- |
74 |
1810 |
| 2E |
- |
4.45 |
70 |
1850 |
| 2F |
1.51 |
2.94 |
56 |
1860 |
[0048] In Tests 2D-2F, the total antifoam concentration was held constant at 4.45 L/tonne.
As observed in Example 1, the combination of silicone and glycol antifoams was synergistic
in terms of the blend addition time and the measured slurry density.
EXAMPLE 3
[0049] In this Example, solid blend composition of Flex I was tested again; however, the
antifoam system consisted of two silicones. One silicone was the same as that used
in the previous examples: the other was an ether functionalized silicone antifoam
(AGOCHEM AF 520, available from CHT Bezema, Tübingen, Germany). The antifoam compositions
and test results are presented in Table 6.
Table 6. Blend addition times and slurry density measurements from Flex I compositions
containing two different silicone antifoam agents.
| Test |
Silicone Antifoam (L/tonne) |
AGOCHEM AF520 (L/tonne) |
Blend Addition Time (s) |
Measured Slurry Density (kg/m3) |
| 3A |
4.45 |
- |
58 |
1820 |
| 3B |
17.8 |
- |
45 |
1900 |
| 3C |
- |
8.9 |
30 |
1930 |
| 3D |
- |
13.3 |
32 |
1940 |
| 3E |
- |
17.8 |
35 |
1940 |
| 3F |
- |
20.5 |
30 |
1960 |
[0050] The results indicate that the functionalized silicone antifoam is more effective
than one used previously, both in terms of blend addition time and measured slurry
density. The results also show how the disclosed mixing method can be used to identify
the optimal antifoam concentration.
EXAMPLE 4
[0051] In this Example, a silicone antifoam was tested in combination with polypropylene
glycols with various molecular weights. The tests were performed with the Flex 2 slurry
composition described earlier. However, the cement was Cemoil Class G instead of Dyckerhoff
Class G. The results are presented in Table 7.

[0052] The least foaming was obtained with the polyethylene glycol that had a molecular
weight of 2000 g/mol. The 400 g/mol polyethylene glycol was the least effective.
[0053] Although only a few example embodiments have been described in detail above, those
skilled in the art will readily appreciate that many modifications are possible in
the example embodiments without materially departing from this disclosure. Accordingly,
all such modifications arc intended to be included within the scope of this disclosure
as defined in the following claims.
1. A well cementing composition, comprising:
(i) an aqueous fluid;
(ii) a solid blend comprising portland cement;
(iii) an air entrainment suppressing agent comprising a blend of a silicone and polypropylene
glycol, or a silicone that is functionalized with ether groups; and
(iv) hydrophobic particles comprising one or more members selected from the list consisting
of rubber particles, polyamides, polypropylene, acrylonitrile butadiene rubbers, polyethylene,
styrene butadiene, uintaite, styrene isoprene styrene (SIS) rubber, styrene isoprene
copolymers, styrene butadiene styrene (SBS) rubber, styrene divinylbenzene, fluoroelastomers,
perfluoroelastomers, polyphenylene sulfide, polyether-etherketone, petroleum coke
derivatives and coal.
2. The composition of claim 1, wherein the silicone/polypropylene glycol blend is present
at a weight ratio between 80% silicone/20% polypropylene glycol and 20% silicone/80%
polypropylene glycol.
3. The composition of claim 1 or 2, wherein the polypropylene glycol has a molecular
weight between 1000 g/mol and 4000 g/mol.
4. The composition of any one of claims 1-3, wherein the silicone/polypropylene glycol
blend is present at a concentration between 4 L/tonne of blend and 40 L/tonne of blend.
5. The composition of any one of claims 1-4, wherein the functionalized silicone is present
at a concentration between 2 L/tonne of blend and 35 L/tonne of blend.
6. The composition of any one of claims 1-5, further comprising latexes or water soluble
polymers or combinations thereof.
7. The composition of claim 6, wherein the latexes comprise styrene butadiene latexes,
carboxylated styrene butadiene latexes, styrene acrylic latexes, acrylic latexes,
isoprene latexes or natural rubber latexes or combinations thereof.
8. The composition of claim 6, wherein the water soluble polymers comprise cellulosic
ethers, acrylates, polymers containing 2-acrylamido-2-methylpropane sulfonic acid
and acrylamides , polysaccharides, polyvinyl alcohols, or crosslinked polyvinyl alcohols
or combinations thereof.
9. A method for preparing a well cementing composition, comprising:
(i) adding an air entrainment suppressing agent to an aqueous fluid, the agent comprising
a blend of a silicone and polypropylene glycol, or a silicone that is functionalized
with ether groups, thereby forming a mixing fluid;
(ii) combining the mixing fluid with a solid blend comprising portland cement in a
continuous process, thereby forming a slurry, wherein the well cementing composition
further comprises hydrophobic particles comprising one or more members selected from
the list consisting of rubber particles, polyamides, polypropylene, acrylonitrile
butadiene rubbers, polyethylene, styrene butadiene, uintaite, styrene isoprene styrene
(SIS) rubber, styrene isoprene copolymers, styrene butadiene styrene (SBS) rubber,
styrene divinylbenzene, fluoroelastomers, perfluoroelastomers, polyphenylene sulfide,
polyether-etherketone, petroleum coke derivatives and coal.
10. The method of claim 9, wherein the silicone/polypropylene glycol blend is present
at a weight ratio between 80% silicone/20% polypropylene glycol and 20% silicone/80%
polypropylene glycol.
11. The method of claim 9 or 10, wherein the polypropylene glycol has a molecular weight
between 1000 g/mol and 4000 g/mol.
12. The method of any one of claims 9-11, wherein the silicone/polypropylene glycol blend
is present at a concentration between 4 L/tonne of blend and 40 L/tonne of blend.
13. The method of any one of claims 9-12, wherein the functionalized silicone is present
at a concentration between 2 L/tonne of blend and 35 L/tonne of blend.
14. The method of any one of claims 9-13, wherein the composition further comprises latexes
or water soluble polymers or combinations thereof.
1. Bohrlochzementierungszusammensetzung, die umfasst:
(i) ein wässriges Fluid;
(ii) eine Portlandzement umfassende feste Mischung;
(iii) ein Luftporenunterdrückungsmittel, das eine Mischung aus einem Silikon und Polypropylenglykol
oder ein mit Ethergruppen funktionalisiertes Silikon umfasst; und
(iv) hydrophobe Partikel, die einen oder mehr Bestandteile ausgewählt aus der Liste
bestehend aus Kautschukpartikeln, Polyamiden, Polypropylen, Acrylnitril-Butadien-Kautschuken,
Polyethylen, Styrol-Butadien, Uintait, Styrol-Isopren-Styrol-(SIS-)Kautschuk, Styrol-Isopren-Copolymeren,
Styrol-Butadien-Styrol-(SBS-)Kautschuk, Styrol-Divinylbenzol, Fluorelastomeren, Perfluorelastomeren,
Polyphenylensulfid, Polyetheretherketon, Petrolkoksderivaten und Kohle umfassen.
2. Zusammensetzung nach Anspruch 1, wobei die Silikon/Polypropylenglykol-Mischung in
einem Gewichtsverhältnis zwischen 80% Silikon/20% Polypropylenglykol und 20% Silikon/80%
Polypropylenglykol vorliegt.
3. Zusammensetzung nach Anspruch 1 oder 2, wobei das Polypropylenglykol ein Molekulargewicht
zwischen 1000 g/mol und 4000 g/mol aufweist.
4. Zusammensetzung nach einem der Ansprüche 1-3, wobei die Silikon/Polypropylenglykol-Mischung
in einer Konzentration zwischen 4 1/t Mischung und 40 1/t Mischung vorliegt.
5. Zusammensetzung nach einem der Ansprüche 1-4, wobei das funktionalisierte Silikon
in einer Konzentration zwischen 2 1/t Mischung und 35 1/t Mischung vorliegt.
6. Zusammensetzung nach einem der Ansprüche 1-5, die ferner Latizes oder wasserlösliche
Polymere oder Kombinationen davon umfasst.
7. Zusammensetzung nach Anspruch 6, wobei die Latizes Styrol-Butadien-Latizes, carboxylierte
Styrol-Butadien-Latizes, Styrol-Acryl-Latizes, Acryl-Latizes, Isopren-Latizes oder
Naturkautschuk-Latizes oder Kombinationen davon umfassen.
8. Zusammensetzung nach Anspruch 6, wobei die wasserlöslichen Polymere Celluloseether,
Acrylate, Polymere enthaltend 2-Acrylamido-2-Methylpropansulfonsäure und Acrylamide,
Polysaccharide, Polyvinylalkohole oder vernetzte Polyvinylalkohole oder Kombinationen
davon umfassen.
9. Verfahren zum Herstellen einer Bohrlochzementierungszusammensetzung, das umfasst:
(i) Zugeben eines Luftporenunterdrückungsmittels zu einem wässrigen Fluid, wobei das
Mittel eine Mischung aus einem Silikon und Polypropylenglykol oder ein mit Ethergruppen
funktionalisiertes Silikon umfasst, wodurch ein Mischfluid ausgebildet wird;
(ii) Kombinieren des Mischfluids mit einer Portlandzement umfassenden festen Mischung
in einem kontinuierlichen Prozess, wodurch eine Aufschlämmung ausgebildet wird, wobei
die Bohrlochzementierungszusammensetzung ferner hydrophobe Partikel umfasst, die einen
oder mehr Bestandteile ausgewählt aus der Liste bestehend aus Kautschukpartikeln,
Polyamiden, Polypropylen, Acrylnitril-Butadien-Kautschuken, Polyethylen, Styrol-Butadien,
Uintait, Styrol-Isopren-Styrol-(SIS-)Kautschuk, Styrol-Isopren-Copolymeren, Styrol-Butadien-Styrol-(SBS-)Kautschuk,
Styrol-Divinylbenzol, Fluorelastomeren, Perfluorelastomeren, Polyphenylensulfid, Polyetheretherketon,
Petrolkoksderivaten und Kohle umfassen.
10. Verfahren nach Anspruch 9, wobei die Silikon/Polypropylenglykol-Mischung in einem
Gewichtsverhältnis zwischen 80% Silikon/20% Polypropylenglykol und 20% Silikon/80%
Polypropylenglykol vorliegt.
11. Verfahren nach Anspruch 9 oder 10, wobei das Polypropylenglykol ein Molekulargewicht
zwischen 1000 g/mol und 4000 g/mol aufweist.
12. Verfahren nach einem der Ansprüche 9-11, wobei die Silikon/Polypropylenglykol-Mischung
in einer Konzentration zwischen 4 1/t Mischung und 40 1/t Mischung vorliegt.
13. Verfahren nach einem der Ansprüche 9-12, wobei das funktionalisierte Silikon in einer
Konzentration zwischen 2 1/t Mischung und 35 1/t Mischung vorliegt.
14. Verfahren nach einem der Ansprüche 9-13, wobei die Zusammensetzung ferner Latizes
oder wasserlösliche Polymere oder Kombinationen davon umfasst.
1. Composition de cimentation de puits, comprenant :
(i) un fluide aqueux;
(ii) un mélange solide comprenant du ciment de Portland ;
(iii) un agent supprimant l'entraînement d'air comprenant un mélange d'un silicone
et de polypropylène glycol, ou un silicone qui est fonctionnalisé avec des groupes
éther ; et
(iv) des particules hydrophobes comprennent un ou plusieurs éléments sélectionnés
dans la liste constituée de particules de caoutchouc, de polyamides, de polypropylène,
de caoutchoucs acrylonitrile-butadiène, de polyéthylène, de styrène butadiène, d'uintahite,
de caoutchouc styrène-isoprène-styrène (SIS), de copolymères styrène-isoprène, de
caoutchouc styrène-butadiène-styrène (SBS), de styrène divinylbenzène, de fluoroélastomères,
de perfluoroélastomères, de sulfure de polyphénylène, de polyéther-éthercétone, de
dérivés de coke de pétrole et de charbon.
2. Composition selon la revendication 1, dans laquelle le mélange silicone/polypropylène
glycol est présent à un rapport de poids entre 80 % silicone / 20 % polypropylène
glycol et 20 % silicone / 80 % polypropylène glycol.
3. Composition selon la revendication 1 ou 2, dans laquelle le polypropylène glycol présente
un poids moléculaire entre 1 000 g/mol et 4 000 g/mol.
4. Composition selon l'une quelconque des revendications 1 à 3, dans laquelle le mélange
silicone/polypropylène glycol est présent à une concentration comprise entre 4 I/tonne
de mélange et 40 I/tonne de mélange.
5. Composition selon l'une quelconque des revendications 1 à 4, dans laquelle le silicone
fonctionnalisé est présent à une concentration comprise entre 2 l/tonne de mélange
et 35 l/tonne de mélange.
6. Composition selon l'une quelconque des revendications 1 à 5, comprenant en outre des
latex ou des polymères hydrosolubles ou des combinaisons de ceux-ci.
7. Composition selon la revendication 6, dans laquelle les latex comprennent des latex
styrène-butadiène, des latex carboxylatés styrène-butadiène, des latex styrène-acrylique,
des latex acrylique, des latex isoprène ou des latex de caoutchouc naturel ou des
combinaisons de ceux-ci.
8. Composition selon la revendication 6, dans laquelle les polymères hydrosolubles comprend
des éthers cellulosiques, des acrylates, des polymères contenant de l'acide 2-acrylamido-2-méthylpropane
sulfonique et des acrylamides, des polysaccharides, des alcools de polyvinyle ou des
alcools de polyvinyle réticulé ou des combinaisons de ceux-ci.
9. Procédé destiné à la préparation d'une composition de cimentation de puits, comprenant
:
(i) l'ajout d'un agent supprimant l'entraînement d'air à un fluide aqueux, l'agent
comprenant un mélange de silicone et de polypropylène glycol, ou un silicone qui est
fonctionnalisé avec des groupes éther ; ce qui permet de former un fluide de mélange
;
(ii) la combinaison du fluide de mélange avec un mélange solide comprenant du ciment
de Portland dans un processus continu, ce qui permet de former une boue, dans lequel
la composition de cimentation de puits comprend en outre des particules hydrophobes
comprenant un ou plusieurs éléments sélectionnés dans la liste constituée de particules
de caoutchouc, de polyamides, de polypropylène, de caoutchoucs acrylonitrile-butadiène,
de polyéthylène, de styrène butadiène, d'uintahite, de caoutchouc styrène-isoprène-styrène
(SIS), de copolymères styrène-isoprène, de caoutchouc styrène-butadiène-styrène (SBS),
de styrène divinylbenzène, de fluoroélastomères, de perfluoroélastomères, de sulfure
de polyphénylène, de polyéther-éthercétone, de dérivés de coke de pétrole et de charbon.
10. Procédé selon la revendication 9, dans lequel le mélange silicone/polypropylène glycol
est présent à un rapport de poids entre 80 % silicone / 20 % polypropylène glycol
et 20 % silicone / 80 % polypropylène glycol.
11. Procédé selon la revendication 9 ou 10, dans lequel le polypropylène glycol présente
un poids moléculaire entre 1 000 g/mol et 4 000 g/mol.
12. Procédé selon l'une quelconque des revendications 9 à 11, dans lequel le mélange silicone/polypropylène
glycol est présent à une concentration comprise entre 4 I/tonne de mélange et 40 I/tonne
de mélange.
13. Procédé selon l'une quelconque des revendications 9 à 12, dans lequel le silicone
fonctionnalisé est présent à une concentration comprise entre 2 I/tonne de mélange
et 35 I/tonne de mélange.
14. Procédé selon l'une quelconque des revendications 9 à 13, dans lequel la composition
comprend en outre des latex ou des polymères hydrosolubles ou des combinaisons de
ceux-ci.